United States · FDA National Drug Code directory
Donepezil Hydrochloride
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 72162-2136_b2bf94c3-a8fe-492e-89c4-a4cdb92001a6
- Product NDC
- 72162-2136
- Form
- TABLET
- Composition / generic term
- Donepezil Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210629
- Source listing expiry
- 20261231
Source-listed ingredients
- DONEPEZIL HYDROCHLORIDE — 5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1000 TABLET in 1 BOTTLE (72162-2136-0) · 72162-2136-0
- 30 TABLET in 1 BOTTLE (72162-2136-3) · 72162-2136-3
- 500 TABLET in 1 BOTTLE (72162-2136-5) · 72162-2136-5
- 90 TABLET in 1 BOTTLE (72162-2136-9) · 72162-2136-9
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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